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Granisetron Hydrochloride
Granisetron Hydrochloride - 51672-4138-0 - (Granisetron Hydrochloride)
Drug Information of Granisetron Hydrochloride
| Product NDC: | 51672-4138 |
| Proprietary Name: | Granisetron Hydrochloride |
| Non Proprietary Name: | Granisetron Hydrochloride |
| Active Ingredient(s): | 1.12 mg/1 & nbsp; Granisetron Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Granisetron Hydrochloride
| Product NDC: | 51672-4138 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090817 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100528 |
Package Information of Granisetron Hydrochloride
| Package NDC: | 51672-4138-0 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (51672-4138-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Granisetron Hydrochloride
| NDC Code | 51672-4138-0 |
| Proprietary Name | Granisetron Hydrochloride |
| Package Description | 10 BLISTER PACK in 1 CARTON (51672-4138-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 51672-4138 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Granisetron Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100528 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | GRANISETRON HYDROCHLORIDE |
| Strength Number | 1.12 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
